(Q54544262)

English

Both temperature and medium composition regulate RNase E processing efficiency of the rpsO mRNA coding for ribosomal protein S15 of Escherichia coli.

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Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/12051911

Both temperature and medium composition regulate RNase E processing efficiency of the rpsO mRNA coding for ribosomal protein S15 of Escherichia coli. (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/12051911

Escherichia coli

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Eliane Hajnsdorf

3

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/12051911

author name string

Le Derout J

1

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/12051911

Régnier P

2

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Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/12051911

language of work or name

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publication date

1 May 2002

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Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/12051911

Journal of Molecular Biology

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Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/12051911

319

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Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/12051911

2

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/12051911

341-349

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/12051911

RNase E, an endoribonuclease, has a general role in the chemical decay of Escherichia coli mRNA: evidence that rne and ams are the same genetic locus

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RNase E: still a wonderfully mysterious enzyme.

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Degradation of mRNA in bacteria: emergence of ubiquitous features

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Structural analysis and in vitro processing to p5 rRNA of a 9S RNA molecule isolated from an rne mutant of E. coli

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A conditional lethal mutation in an Escherichia coli strain with a longer chemical lifetime of messenger RNA

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RNase G (CafA protein) and RNase E are both required for the 5' maturation of 16S ribosomal RNA.

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Decay of mRNA encoding ribosomal protein S15 of Escherichia coli is initiated by an RNase E-dependent endonucleolytic cleavage that removes the 3' stabilizing stem and loop structure

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Specific endonucleolytic cleavage of the mRNA for ribosomal protein S20 of Escherichia coli requires the product of the ams gene in vivo and in vitro

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RNase E autoregulates its synthesis by controlling the degradation rate of its own mRNA in Escherichia coli: unusual sensitivity of the rne transcript to RNase E activity.

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The rate of processing and degradation of antisense RNAI regulates the replication of ColE1-type plasmids in vivo

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Regulation of plasmid R1 replication: PcnB and RNase E expedite the decay of the antisense RNA, CopA

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Sok antisense RNA from plasmid R1 is functionally inactivated by RNase E and polyadenylated by poly(A) polymerase I

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Control of RNase E-mediated RNA degradation by 5'-terminal base pairing in E. coli

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Stabilization of circular rpsT mRNA demonstrates the 5'-end dependence of RNase E action in vivo

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Ribosomes inhibit an RNase E cleavage which induces the decay of the rpsO mRNA of Escherichia coli.

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mRNAs can be stabilized by DEAD-box proteins

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Autoregulation allows Escherichia coli RNase E to adjust continuously its synthesis to that of its substrates

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RNase E, the major player in mRNA degradation, is down-regulated in Escherichia coli during a transient growth retardation (diauxic lag)

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Decay of ompA mRNA and processing of 9S RNA are immediately affected by shifts in growth rate, but in opposite manners

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7 January 2021

Roles of RNase E, RNase II and PNPase in the degradation of the rpsO transcripts of Escherichia coli: stabilizing function of RNase II and evidence for efficient degradation in an ams pnp rnb mutant.

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Polynucleotide phosphorylase is required for the rapid degradation of the RNase E-processed rpsO mRNA of Escherichia coli devoid of its 3' hairpin.

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Ribosomal protein S15 from Escherichia coli modulates its own translation by trapping the ribosome on the mRNA initiation loading site.

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Multiple degradation pathways of the rpsO mRNA of Escherichia coli. RNase E interacts with the 5' and 3' extremities of the primary transcript.

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Regulation of the synthesis of ribosomes and ribosomal components

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Diverse mechanisms for regulating ribosomal protein synthesis in Escherichia coli

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inferred from DOI database lookup

Stabilization of the 3' one-third of Escherichia coli ribosomal protein S20 mRNA in mutants lacking polynucleotide phosphorylase

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7 January 2021

Differential sensitivities of portions of the mRNA for ribosomal protein S20 to 3'-exonucleases dependent on oligoadenylation and RNA secondary structure.

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Processing of the rne transcript by an RNase E-independent amino acid-dependent mechanism.

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The C-terminal half of RNase E, which organizes the Escherichia coli degradosome, participates in mRNA degradation but not rRNA processing in vivo

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Analysis of mRNA decay and rRNA processing in Escherichia coli in the absence of RNase E-based degradosome assembly

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RNase E polypeptides lacking a carboxyl-terminal half suppress a mukB mutation in Escherichia coli

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Role of the heat shock response in stability of mRNA in Escherichia coli K-12

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mRNA degradation. A tale of poly(A) and multiprotein machines.

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Degradation of mRNA in Escherichia coli: an old problem with some new twists

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Nucleolytic inactivation and degradation of the RNase III processed pnp message encoding polynucleotide phosphorylase of Escherichia coli

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Identifiers

10.1016/S0022-2836(02)00295-4

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/12051911

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 May 2018

http://europepmc.org/abstract/MED/12051911

ResearchGate publication ID

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